Canonical Allele Identifier: CA2774715068

Gene: KLHL7

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.23165975_23165976insACTC , CM000669.2:g.23165975_23165976insACTC	GRCh38
NC_000007.13:g.23205594_23205595insACTC , CM000669.1:g.23205594_23205595insACTC	GRCh37
NC_000007.12:g.23172119_23172120insACTC	NCBI36
NG_016983.1:g.65242_65243insACTC
NG_016983.2:g.65242_65243insACTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339077.10:c.1177+37_1177+38insACTC MANE Select	ENSP00000343273.4:n.1177+37_1177+38insACTC
ENST00000339077.9:c.1177+37_1177+38insACTC	ENSP00000343273.4:n.1177+37_1177+38insACTC
ENST00000409689.5:c.1033+37_1033+38insACTC	ENSP00000386263.1:n.1033+37_1033+38insACTC
ENST00000469576.1:n.64+37_64+38insACTC
ENST00000521082.5:c.*1185+37_*1185+38insACTC	ENSP00000430351.1:n.*1185+37_*1185+38insACTC
NM_001031710.2:c.1177+37_1177+38insACTC	NP_001026880.2:n.1177+37_1177+38insACTC
NM_018846.4:c.1033+37_1033+38insACTC	NP_061334.4:n.1033+37_1033+38insACTC
NR_033328.1:n.1601+37_1601+38insACTC
XM_006715753.1:c.1216+37_1216+38insACTC	XP_006715816.1:n.1216+37_1216+38insACTC
XM_006715754.1:c.1150+37_1150+38insACTC	XP_006715817.1:n.1150+37_1150+38insACTC
XM_006715755.1:c.1150+37_1150+38insACTC	XP_006715818.1:n.1150+37_1150+38insACTC
XM_006715756.1:c.1072+37_1072+38insACTC	XP_006715819.1:n.1072+37_1072+38insACTC
XM_006715753.3:c.1216+37_1216+38insACTC	XP_006715816.1:n.1216+37_1216+38insACTC
XM_006715754.3:c.1150+37_1150+38insACTC	XP_006715817.1:n.1150+37_1150+38insACTC
XM_006715755.3:c.1150+37_1150+38insACTC	XP_006715818.1:n.1150+37_1150+38insACTC
XM_006715756.3:c.1072+37_1072+38insACTC	XP_006715819.1:n.1072+37_1072+38insACTC
XM_017012439.2:c.1111+37_1111+38insACTC	XP_016867928.1:n.1111+37_1111+38insACTC
NM_001031710.3:c.1177+37_1177+38insACTC MANE Select	NP_001026880.2:n.1177+37_1177+38insACTC
NM_018846.5:c.1033+37_1033+38insACTC	NP_061334.4:n.1033+37_1033+38insACTC
NR_033328.2:n.1550+37_1550+38insACTC